ORCID Profile
0000-0002-9702-6949
Current Organisation
Università degli Studi di Milano
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Publisher: Elsevier BV
Date: 2013
Publisher: Elsevier BV
Date: 2012
DOI: 10.1016/J.ULTSONCH.2011.05.018
Abstract: An ultrasound-assisted method was used for synthesizing nanosized Pt-graphene oxide (GO)-TiO2 photocatalyst. The Pt-GO-TiO2 nanoparticles were characterized by diffused reflectance spectroscopy, X-ray diffraction, N2 BET adsorption-desorption measurements, atomic force microscopy and transmission electron microscopy. The photocatalytic and sonophotocatalytic degradation of a commonly used anionic surfactant, dodecylbenzenesulfonate (DBS), in aqueous solution was carried out using Pt-GO-TiO2 nanoparticles in order to evaluate the photocatalytic efficiency. For comparison purpose, sonolytic degradation of DBS was carried out. The Pt-GO-TiO2 catalyst degraded DBS at a higher rate than P-25 (TiO2), prepared TiO2 or GO-TiO2 photocatalysts. The mineralization of DBS was enhanced by a factor of 3 using Pt-GO-TiO2 compared to the P-25 (TiO2). In the presence of GO, an enhanced rate of DBS oxidation was observed and, when doped with platinum, mineralization of DBS was further enhanced. The Pt-GO-TiO2 catalyst also showed a considerable amount of degradation of DBS under visible light irradiation. The initial solution pH had an effect on the rate of photocatalytic oxidation of DBS, whereas no such effect of initial pH was observed in the sonochemical or sonophotocatalytic oxidation of DBS. The intermediate products formed during the degradation of DBS were monitored using electrospray mass spectrometry. The ability of GO to serve as a solid support to anchor platinum particles on GO-TiO2 is useful in developing new photocatalysts.
Publisher: Elsevier BV
Date: 06-2016
DOI: 10.1016/J.CHEMOSPHERE.2016.03.063
Abstract: TiO2-encapsulated H-ZSM photocatalysts were prepared by physical mixing of TiO2 and zeolites. Pt was immobilized on the surface of the TiO2-encapsulated zeolite (H-ZSM) catalysts by a simple photochemical reduction method. Different weight ratios of both TiO2 and Pt were hybridized with H-ZSM and the catalytic performance of the prepared catalysts was investigated for 2-propanol oxidation in liquid phase and acetaldehyde in gas phase reaction. Around 5-10 wt% TiO2-encapsulated H-ZSM catalysts was found to be optimal amount for the effective oxidation of the organics. Prior to light irradiation, Pt-TiO2-H-ZSM showed considerable amount of catalytic degradation of 2-propanol in the dark, forming acetone as an intermediate. In this study, Pt has played a major and important role on the total oxidation of 2-propanol as well as acetaldehyde. As a result, no residual organics were present in the pores of the zeolites. The catalysts could be reused more than three times without losing their catalytic activity in both phases. The Pt-TiO2-H-ZSM photocatalysts could overcome the problem of strong adsorption of organics in the zeolite pores (after the reaction). Thus, Pt-TiO2-H-ZSM can be used as a potential catalyst for both liquid and gas phase oxidation of organic pollutants.
Publisher: MDPI AG
Date: 03-09-2018
DOI: 10.3390/NANO8090686
Abstract: TiO2-based photocatalysis under visible light is an attractive way to abate air pollutants. Moreover, developing photocatalytic materials on a large-scale requires safe and low-cost precursors. Both high-performance TiO2 nanopowders and visible-light active noble metals do not match these requirements. Here, we report the design of novel Mn-decorated micrometric TiO2 particles. Pigmentary TiO2 replaced unsafe nano-TiO2 and firmly supported MnOx particles. Mn replaced noble metals such as Au or Ag, opening the way for the development of lower cost catalysts. Varying Mn loading or pH during the impregnation affected the final activity, thus giving important information to optimize the synthesis. Photocatalytic activity screening occurred on the gas-phase degradation of ethanol as a reference molecule, both under ultraviolet (UV) (6 h) and Light Emitting Diode (LED) (24 h) irradiation. Mn-doped TiO2 reached a maximum ethanol degradation of 35% under visible light after 24 h for the s le containing 20% of Mn. Also, we found that an acidic pH increased both ethanol degradation and mineralization to CO2, while an alkaline pH drastically slowed down the reaction. A strict correlation between photocatalytic results and physico-chemical characterizations of the synthesized powders were drawn.
Publisher: American Scientific Publishers
Date: 06-2015
Publisher: Elsevier BV
Date: 2018
DOI: 10.1016/J.ULTSONCH.2017.07.016
Abstract: Titanium dioxide is the most popular photocatalyst to degrade organic pollutants in air, as well as in water. The principal drawback preventing its commercial application lies in its limited absorption of the visible light (400-700nm), while it is active under UV irradiation (≤387nm). Supporting noble metals in the form of nanoparticles on TiO
Publisher: Elsevier BV
Date: 2011
DOI: 10.1016/J.ULTSONCH.2010.04.002
Abstract: The oxidative degradation of 4-chlorophenol (4-CP) by sonolytic, photocatalytic and sonophotocatalytic processes was studied in aqueous solutions using Bi(2)O(3)/TiZrO(4) as a visible light driven photocatalyst and with 20 kHz ultrasound. The results reveal that Bi(2)O(3)/TiZrO(4) is an efficient photocatalyst capable of degrading 4-CP by both photocatalytic and sonophotocatalytic processes. During the sonolysis of 4-CP solutions, HPLC results showed the formation of a number of intermediate products, whereas, no such intermediates were formed during the sonophotocatalytic degradation of 4-CP. TOC results showed rapid mineralization of 4-CP during the sonophotocatalytic degradation process, relative to that observed with sonolysis alone. The results reveal a clear advantage in using a coupled method for the oxidation of 4-CP and a cumulative effect was observed. Further, the solution pH had no specific influence on the sonophotocatalytic degradation of 4-CP, unlike the situation for sonolysis alone where the degradation rate decreased as the pH was raised from acidic to basic conditions. The combined sonophotocatalytic degradation process was found to be simple to apply and has the potential to be a powerful method for the remediation of organic contaminants present in water and wastewater.
No related grants have been discovered for Claudia Bianchi.